TriMed Dorsal Wrist Hook Plate — Class II medical device recall Z-0118-2020
Terminated recall by TriMed Inc., reported 2019-10-16, distributed in CA, FL, MD, TX, WA. Modifications to the specification were not appropriately qualified through the company's design control proce
| Recall number | Z-0118-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | TriMed Inc., Santa Clarita, CA, United States |
| Recall initiated | 2018-08-24 |
| Classified | 2019-10-10 |
| Reported by FDA | 2019-10-16 |
| Terminated | 2021-04-28 |
| Distributed | CA, FL, MD, TX, WA |
| Countries outside the US | AU |
| Quantity | 5 devices |
| Lot numbers | 28884, 28885, 28886, 28887 |
| Model numbers | WHD-4 |
Product
TriMed Dorsal Wrist Hook Plate, Dorsal, 4-Hole, REF WHD-4, contained in a tray, insert, or poly package containing varying amounts, Nonsterile, Single Use Only, Rx. The firm name on the label is TriMed, Santa Clarita, CA.
Reason for recall
Modifications to the specification were not appropriately qualified through the company's design control process which may result in structural integrity issues of the device.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0118-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.